Primary alkynes R′CCH [R′ = Me3Si, Tol, CH2OH, CO2Me, (CH2)4CCH, Me] insert intothe metal–carbon bond ofdiruthenium μ-aminocarbynes [Ru2{μ-CN(Me)(R)}(μ-CO)(CO)(MeCN)(Cp)2][SO3CF3] [R = 2,6-Me2C6H3 (Xyl), 1a; CH2Ph (Bz), 1b; Me, 1c] to give thevinyliminiumcomplexes [Ru2{μ-η1:η3-C(R′)CHCN(Me)(R)}(μ-CO)(CO)(Cp)2][SO3CF3] [R = Xyl, R′ = Me3Si, 2a; R = Bz, R′ = Me3Si, 2b; R = Me, R′ = Me3Si, 2c; R = Xyl, R′ = Tol, 3a; R = Bz, R′ = Tol, 3b; R = Bz, R′ = CH2OH, 4; R = Bz, R′ = CO2Me, 5a; R = Me, R′ = CO2Me, 5b; R = Xyl, R′ = (CH2)4CCH, 6; R = Xyl, R′ = Me, 7a; R = Bz, R′ = Me, 7b; R = Me, R′ = Me, 7c]. The related compound [Ru2{μ-η1:η3-C[C(Me)CH2]CHCN(Me)(Xyl)}(μ-CO)(CO)(Cp)2][SO3CF3], (9) is better prepared by reacting [Ru2{μ-CN(Me)(Xyl)}(μ-CO)(CO)(Cl)(Cp)2] (8) with AgSO3CF3 in the presence of HCCC(Me)CH2 in CH2Cl2 at low temperature.In a similar way, also secondary alkynes can be inserted to give thenewcomplexes [Ru2{μ-η1:η3-C(R′)C(R′)CN(Me)(R)}(μ-CO)(CO)(Cp)2][SO3CF3] (R = Bz, R′ = CO2Me, 11; R = Xyl, R′ = Et, 12a; R = Bz, R′ = Et, 12b; R = Xyl, R′ = Me, 13). The reactions of2–7, 9, 11–13 with hydrides (i.e., NaBH4, NaH) have been also studied, affording μ-vinylalkylidene complexes [Ru2{μ-η1:η3-C(R′)C(R″)C(H)N(Me)(R)}(μ-CO)(CO)(Cp)2] (R = Bz, R′ = Me3Si, R″ = H, 14a; R = Me, R′ = Me3Si, R″ = H, 14b; R = Bz, R′ = Tol, R″ = H, 15; R = Bz, R′ = R″ = Et, 16), bis-alkylidene complexes [Ru2{μ-η1:η2-C(R′)C(H)(R″)CN(Me)(Xyl)}(μ-CO)(CO)(Cp)2] (R′ = Me3Si, R″ = H, 17; R′ = R″ = Et, 18), acetylide compounds [Ru2{μ-CN(Me)(R)}(μ-CO)(CO)(CCR′)(Cp)2] (R = Xyl, R′ = Tol, 19; R = Bz, R′ = Me3Si, 20; R = Xyl, R′ = Me, 21) or the tetranuclear species [Ru2{μ-η1:η2-C(Me)CCN(Me)(Bz)}(μ-CO)(CO)(Cp)2]2 (23) depending on the properties ofthe hydride and the substituents on thecomplex. Chromatography of21 on alumina results in its conversion into [Ru2{μ-η3:η1-C[N(Me)(Xyl)]C(H)CCH2}(μ-CO)(CO)(Cp)2] (22). The crystal structures of2a[CF3SO3] · 0.5CH2Cl2, 12a[CF3SO3] and 22 have been determined by X-ray diffraction studies.

New diruthenium vinyliminium complexes from the insertion of alkynes into bridging aminocarbynes

MARCHETTI, FABIO;
2006-01-01

Abstract

Primary alkynes R′CCH [R′ = Me3Si, Tol, CH2OH, CO2Me, (CH2)4CCH, Me] insert intothe metal–carbon bond ofdiruthenium μ-aminocarbynes [Ru2{μ-CN(Me)(R)}(μ-CO)(CO)(MeCN)(Cp)2][SO3CF3] [R = 2,6-Me2C6H3 (Xyl), 1a; CH2Ph (Bz), 1b; Me, 1c] to give thevinyliminiumcomplexes [Ru2{μ-η1:η3-C(R′)CHCN(Me)(R)}(μ-CO)(CO)(Cp)2][SO3CF3] [R = Xyl, R′ = Me3Si, 2a; R = Bz, R′ = Me3Si, 2b; R = Me, R′ = Me3Si, 2c; R = Xyl, R′ = Tol, 3a; R = Bz, R′ = Tol, 3b; R = Bz, R′ = CH2OH, 4; R = Bz, R′ = CO2Me, 5a; R = Me, R′ = CO2Me, 5b; R = Xyl, R′ = (CH2)4CCH, 6; R = Xyl, R′ = Me, 7a; R = Bz, R′ = Me, 7b; R = Me, R′ = Me, 7c]. The related compound [Ru2{μ-η1:η3-C[C(Me)CH2]CHCN(Me)(Xyl)}(μ-CO)(CO)(Cp)2][SO3CF3], (9) is better prepared by reacting [Ru2{μ-CN(Me)(Xyl)}(μ-CO)(CO)(Cl)(Cp)2] (8) with AgSO3CF3 in the presence of HCCC(Me)CH2 in CH2Cl2 at low temperature.In a similar way, also secondary alkynes can be inserted to give thenewcomplexes [Ru2{μ-η1:η3-C(R′)C(R′)CN(Me)(R)}(μ-CO)(CO)(Cp)2][SO3CF3] (R = Bz, R′ = CO2Me, 11; R = Xyl, R′ = Et, 12a; R = Bz, R′ = Et, 12b; R = Xyl, R′ = Me, 13). The reactions of2–7, 9, 11–13 with hydrides (i.e., NaBH4, NaH) have been also studied, affording μ-vinylalkylidene complexes [Ru2{μ-η1:η3-C(R′)C(R″)C(H)N(Me)(R)}(μ-CO)(CO)(Cp)2] (R = Bz, R′ = Me3Si, R″ = H, 14a; R = Me, R′ = Me3Si, R″ = H, 14b; R = Bz, R′ = Tol, R″ = H, 15; R = Bz, R′ = R″ = Et, 16), bis-alkylidene complexes [Ru2{μ-η1:η2-C(R′)C(H)(R″)CN(Me)(Xyl)}(μ-CO)(CO)(Cp)2] (R′ = Me3Si, R″ = H, 17; R′ = R″ = Et, 18), acetylide compounds [Ru2{μ-CN(Me)(R)}(μ-CO)(CO)(CCR′)(Cp)2] (R = Xyl, R′ = Tol, 19; R = Bz, R′ = Me3Si, 20; R = Xyl, R′ = Me, 21) or the tetranuclear species [Ru2{μ-η1:η2-C(Me)CCN(Me)(Bz)}(μ-CO)(CO)(Cp)2]2 (23) depending on the properties ofthe hydride and the substituents on thecomplex. Chromatography of21 on alumina results in its conversion into [Ru2{μ-η3:η1-C[N(Me)(Xyl)]C(H)CCH2}(μ-CO)(CO)(Cp)2] (22). The crystal structures of2a[CF3SO3] · 0.5CH2Cl2, 12a[CF3SO3] and 22 have been determined by X-ray diffraction studies.
2006
L., Busetto; Marchetti, Fabio; S., Zacchini; V., Zanotti
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11568/181922
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